The Safety Rates Drug Report

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Drug     Injury     Quarter    

Person who experienced the adverse event (patient)

Event ID CASE I F COD FOLL SEQ IMAGE EVENT DT MFR DT FDA DT REPT COD MFR NUM MFR SNDR AGE AGE COD GNDR COD E SUB WT WT COD REPT DT OCCP COD DEATH DT TO MFR CONFID REPORTER COUNTRY
7233449 8169160 I 7233449-2 20040922 20110110 20110119 EXP FR-PFIZER INC-2005006536 PFIZERINC 59 YR F Y 57 KG 20110119 OT FRANCE

Drug(s) used by person

Event ID DRUG SEQ ROLE COD DRUGNAME VAL VBM ROUTE DOSE VBM DECHAL RECHAL LOT NUM EXP DT NDA NUM
7233449 1015555410 SS FLUOROURACIL 1 INTRAVENOUS 800 MG, CYCLIC 040023
7233449 1015555411 SS CYCLOPHOSPHAMIDE 1 INTRAVENOUS 800 MG, CYCLIC
7233449 1015555413 SS FILGRASTIM 2 SUBCUTANEOUS
7233449 1015555409 PS EPIRUBICIN HYDROCHLORIDE 1 INTRAVENOUS 170 MG, CYCLIC 50778
7233449 1015555412 SS DEXRAZOXANE 1 INTRAVENOUS 1700 MG, CYCLIC
7233449 1015555414 SS ZOLEDRONIC ACID 1 INTRAVENOUS

Indications of drugs used

Event ID DRUG SEQ INDI PT
7233449 1015555410 BREAST CANCER
7233449 1015555411 BREAST CANCER
7233449 1015555413 AGRANULOCYTOSIS
7233449 1015555409 BREAST CANCER
7233449 1015555412 BREAST CANCER
7233449 1015555414 ILL-DEFINED DISORDER

Outcome of event

Event ID OUTC COD
7233449 HO

Reactions reported

Event ID PT
7233449 HYPOPHOSPHATAEMIA
7233449 PROTEINURIA
7233449 HYPOKALAEMIA
7233449 RENAL TUBULAR DISORDER

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

Event ID DRUG SEQ START DT END DT DUR DUR COD
7233449 1015555410 20040726 20040726 1 DAY
7233449 1015555411 20040726 20040726 1 DAY
7233449 1015555409 20040726 20040726 1 DAY
7233449 1015555412 20040726 20040726 1 DAY
7233449 1015555414 20040821